The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
Role of septal vasopressin innervation in paternal behavior in prairie voles (Microtus ochrogaster).
Open accessAbstract
After being paired with females, male prairie voles show major changes in their social behaviors among which is an increase in paternal responsiveness. These changes are accompanied by fluctuations in the density of the [Arg8]vasopressin-immunoreactive (AVP-ir) fibers in the lateral septum, suggesting that septal AVP might be involved in these changes. To explore a possible involvement of septal AVP in paternal responsiveness, we tested whether injections of saline, AVP, or the V1a receptor antagonist [1-(beta-mercapto-beta, beta-cyclopentamethylenepropionic acid),2-(O-methyltyrosine]AVP [d(CH2)5Tyr(Me)AVP] into the lateral septum influenced the four most prominent paternal activities displayed by male prairie voles; grooming, crouching over, contacting, and retrieving pups. In a first experiment, sexually inexperienced males received a single injection of AVP, saline, or d(CH2)5Tyr(Me)AVP in the lateral septum, after which their paternal responsiveness was recorded during a 10-min period. AVP-injected animals spent more time contacting and crouching over pups, while d(CH2)5Tyr(Me)AVP-injected animals spent less time grooming pups than saline-injected animals. In a follow-up study, one group of animals received an injection of AVP preceded by an injection of saline or d(CH2)5Tyr(Me)-AVP into the lateral septum. A second group of animals received an injection of saline preceded by an injection of saline or d(CH2)5Tyr(Me)AVP into the lateral septum. In both groups, animals spent less time grooming, crouching over, and contacting pups if they had first been injected with d(CH2)5Tyr(Me)AVP. Control experiments suggested that the effects of AVP on paternal responsiveness were dose- and site-specific. These data suggest that septal AVP enhances paternal responsiveness by a V1a receptor-mediated mechanism.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“The influence of AVP on male parental behavior in prairie voles is localized to the lateral septum (LS), where local AVPR1a stimulation or blockade respectively increases or decreases paternal behavior [48].”
From The Neurobiology of Love and Pair Bonding from Human and Animal Perspectives (2023) · cites this paper as [48]
The cited source says what the claim attributes to it.
In the citing paper
“In addition to the effects of OT and DA in promoting parental care of both sexes, AVP, known to promote territoriality, aggression, and mating, has been linked to parental nurturing [48,49,50,51].”
From The Neurobiology of Love and Pair Bonding from Human and Animal Perspectives (2023) · cites this paper as [48]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Rodent studies of mating suggest a sexually dimorphic role of AVP in sexual behavior.”
From The Neurobiology of Love and Pair Bonding from Human and Animal Perspectives (2023) · cites this paper as [48]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“In male but not female mice, AVP cells in the BNST and MeA are active during mating, and the knockdown of BNST AVP cells inhibits male sexual behaviors [48,51].”
From The Neurobiology of Love and Pair Bonding from Human and Animal Perspectives (2023) · cites this paper as [48]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“For example, AVP mRNA expression in BNST neurons increased following mating in male, but not female, prairie voles (Wang, Ferris, & De Vries, 1994).”
From Quantitative mapping reveals age and sex differences in vasopressin, but not oxytocin, immunoreactivity in the rat social behavior neural network (2017) · cites this paper as Wang et al., 1994
Experimental — accuracy not yet measured
In the citing paper
“AVP injected into the LS increases, while V1aR antagonist decreases, paternal behavior in male prairie voles (Wang et al 1994).”
From The behavioral, anatomical and pharmacological parallels between social attachment, love and addiction (2012) · cites this paper as Wang et al 1994
In the citing paper
“AVP induces pair bonding in male prairie voles when injected into the LS, and V1aR antagonist in the LS or the ventral pallidum (VP) prevents pair bonding (Wang et al 1994; Lim and Young 2004).”
From The behavioral, anatomical and pharmacological parallels between social attachment, love and addiction (2012) · cites this paper as Wang et al 1994
In the citing paper
“Infusion of AVP into the lateral septum increased paternal behaviors, while an AVPR1A antagonist decreased time spent tending the pups [38].”
From The prairie vole: An emerging model organism for understanding the social brain (2010) · cites this paper as [38]
In the citing paper
“Infusion of AVP into the lateral septum increased paternal behaviors, while an AVPR1A antagonist decreased time spent tending the pups [38].”
From The prairie vole: An emerging model organism for understanding the social brain (2010) · cites this paper as [38]
In the citing paper
“Although the precise sources of AVP regulating parental behavior is undefined, AVP projections from the extended amygdala may also influence maternal behavior, as AVP in the LS facilitates paternal behavior in prairie voles (135, 136).”
From Oxytocin, Vasopressin, and Social Behavior: From Neural Circuits to Clinical Opportunities (2022) · cites this paper as [135]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A role for central vasopressin in pair bonding in monogamous prairie voles
Winslow, J. T., Hastings, N., Carter, C. S., Harbaugh, C. R., & Insel, T. R. (1993) · Nature · doi:10.1038/365545a0 · Cited by 948
Oxytocin receptor distribution reflects social organization in monogamous and polygamous voles
Insel, T. R., & Shapiro, L. E. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5981 · Cited by 833
Oxytocin induces maternal behavior in virgin female rats
Pedersen, C. A., Ascher, J. A., Monroe, Y. L., & Prange, A. J. (1982) · Science · doi:10.1126/science.7071605 · Cited by 770
de Vries, G. J., & Buijs, R. M. (1983) · Brain Research · doi:10.1016/0006-8993(83)90855-7 · Cited by 524
The vasopressinergic innervation of the brain in normal and castrated rats
DeVries, G. J., Buijs, R. M., van Leeuwen, F. W., Caffé, A. R., & Swaab, D. F. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902330206 · Cited by 522
Kruszynski, M., Lammek, B., Manning, M., Seto, J., Haldar, J., & Sawyer, W. H. (1980) · Journal of Medicinal Chemistry · doi:10.1021/jm00178a003 · Cited by 450
De Vries, G. J., Buds, R. M., & Swaab, D. F. (1981) · Brain Research · doi:10.1016/0006-8993(81)90989-6 · Cited by 319
Caffé, A. R., van Leeuwen, F. W., & Luiten, P. G. M. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902610206 · Cited by 286
Bamshad, M., Novak, M. A., & De Vries, G. J. (1993) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1993.tb00480.x · Cited by 175
Prolactin and paternal behavior in the biparental California mouse, Peromyscus californicus
Gubernick, D. J., & Nelson, R. J. (1989) · Hormones and Behavior · doi:10.1016/0018-506x(89)90061-5 · Cited by 167
Cited by
Sorted by citations
Items 201–300 of 387
lqbal, J., Swanson, J. J., Prins, G. S., & Jacobson, C. D. (1995) · Brain Research · doi:10.1016/0006-8993(95)00983-3 · Cited by 43
Male-female associations and female olfactory neurogenesis with pair bonding in Mus spicilegus
Baudoin, C., Busquet, N., Dobson, F. S., Gheusi, G., Féron, C., Durand, J., Heth, G., Patris, B., & Todrank, J. (2005) · Biological Journal of the Linnean Society · doi:10.1111/j.1095-8312.2005.00437.x · Cited by 42
Tanaka, K., Suzuki, M., Sumiyoshi, T., Murata, M., Tsunoda, M., & Kurachi, M. (2003) · Brain Research · doi:10.1016/j.brainres.2003.08.050 · Cited by 42
Wang, Z., & Insel, T. R. (1996) · Advances in the study of behavior · doi:10.1016/s0065-3454(08)60338-1 · Cited by 41
Self-citationHayes, U. L., & Vries, G. J. D. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.10.011 · Cited by 41
Prolactin Action Is Necessary for Parental Behavior in Male Mice
Smiley, K. O., Brown, R. S. E., & Grattan, D. R. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0558-22.2022 · Cited by 41
Hostetler, C. M., Hinde, K., Maninger, N., Mendoza, S. P., Mason, W. A., Rowland, D. J., Wang, G. B., Kukis, D. L., Cherry, S. R., & Bales, K. L. (2016) · American Journal of Primatology · doi:10.1002/ajp.22612 · Cited by 40
Intranasal oxytocin modulates neural functional connectivity during human social interaction
Rilling, J. K., Chen, X., Chen, X., & Haroon, E. (2018) · American Journal of Primatology · doi:10.1002/ajp.22740 · Cited by 40
The parental brain: Transformations and adaptations
Lambert, K. G. (2012) · Physiology & Behavior · doi:10.1016/j.physbeh.2012.03.018 · Cited by 40
Kelly, A. M., & Goodson, J. L. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.09.006 · Cited by 38
Klatt, J. D., & Goodson, J. L. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.10.001 · Cited by 38
Glucocorticoid regulation of vasopressin V1a receptors in rat forebrain
Watters, J. J., Wilkinson, C. W., & Dorsa, D. M. (1996) · Molecular Brain Research · doi:10.1016/0169-328x(95)00345-s · Cited by 39
Liu, Y., Donovan, M. L., Jia, X., & Wang, Z. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14550 · Cited by 38
Self-citationWoller, M. J., Sosa, M. E., Chiang, Y., Prudom, S. L., Keelty, P., Moore, J. E., & Ziegler, T. E. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02252.x · Cited by 39
Jones, J. S., & Wynne‐Edwards, K. E. (2001) · Animal Behaviour · doi:10.1006/anbe.2001.1765 · Cited by 38
Fatherhood Alters Behavioural and Neural Responsiveness in a Spatial Task
Franssen, C. L., Bardi, M., Shea, E. A., Hampton, J. E., Franssen, R. A., Kinsley, C. H., & Lambert, K. G. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02225.x · Cited by 36
Pair bonds and parental behaviour
McGraw, L. A., Székely, T., & Young, L. J. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511781360.023 · Cited by 37
Hostetler, C. M., Hitchcock, L. N., Anacker, A. M. J., Young, L. J., & Ryabinin, A. E. (2012) · Peptides · doi:10.1016/j.peptides.2012.12.008 · Cited by 34
Ni, R., Shu, Y., Wang, J., Yin, J. C. P., Xu, L., & Zhou, J. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.034 · Cited by 33
Vries, G. J. D., AL‐SHAMMA, H. A., & ZHOU, L. (1994) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1994.tb55789.x · Cited by 34
A, T. R. D. J., Kőrösi, A., Harris, B. N., Perea-Rodríguez, J. P., & Wendy Saltzman, A. (2012) · Physiological and Biochemical Zoology · doi:10.1086/665831 · Cited by 33
Albers, H. E., & Cooper, T. T. (1995) · Peptides · doi:10.1016/0196-9781(94)00188-x · Cited by 33
Effects of vasopressin on neural processing of infant crying in expectant fathers
Thijssen, S., Van 't Veer, A. E., Witteman, J., Meijer, W. M., van IJzendoorn, M. H., & Bakermans-Kranenburg, M. J. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.05.014 · Cited by 31
Klampfl, S. M., Brunton, P. J., Bayerl, D. S., & Bosch, O. J. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.11.015 · Cited by 32
Planas, B., Kolb, P. E., Raskind, M. A., & MILLER, M. A. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903610105 · Cited by 32
Rogers Flattery, C. N., Coppeto, D. J., Inoue, K., Rilling, J. K., Preuss, T. M., & Young, L. J. (2022) · Brain Structure and Function · doi:10.1007/s00429-021-02369-7 · Cited by 31
Sexual Dimorphism of Parental Care: From Genes to Behavior
Zilkha, N., Scott, N., & Kimchi, T. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031447 · Cited by 33
Oxytocin Neurons Exhibit Extensive Functional Plasticity Due To Offspring Age in Mothers and Fathers
Kelly, A. M., Hiura, L. C., Saunders, A. G., & Ophir, A. G. (2017) · Integrative and Comparative Biology · doi:10.1093/icb/icx036 · Cited by 30
Sadino, J. M., & Donaldson, Z. R. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.7b00475 · Cited by 30
Stoesz, B. M., Hare, J. F., & Snow, W. M. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.11.007 · Cited by 28
Neuroendocrinology and Adaptive Physiology of Maternal Care
Smiley, K. O., Ladyman, S. R., Gustafson, P. E., Grattan, D. R., & Brown, R. S. E. (2019) · Current topics in behavioral neurosciences · doi:10.1007/7854_2019_122 · Cited by 28
Oldfield, R. G., Harris, R. M., & Hofmann, H. A. (2015) · Frontiers in Zoology · doi:10.1186/1742-9994-12-s1-s16 · Cited by 28
MILLER, M. A., Kolb, P. E., & Raskind, M. A. (1997) · Molecular Brain Research · doi:10.1016/s0169-328x(97)00250-7 · Cited by 27
Ophir, A. G., Crino, O. L., Wilkerson-Vidal, Q. C., Wolff, J. O., & Phelps, S. M. (2007) · Brain Behavior and Evolution · doi:10.1159/000108609 · Cited by 26
Gene Regulation as a Modulator of Social Preference in Voles
Hammock, E. A. D. (2007) · Advances in genetics · doi:10.1016/s0065-2660(07)59004-8 · Cited by 26
The role of oxytocin and vasopressin in conditioned mate guarding behavior in the female rat
Holley, A., Bellevue, S., Vosberg, D., Wenzel, K., Roorda, S., & Pfaus, J. G. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.02.039 · Cited by 28
Rigney, N., Campos‐Lira, E., Kirchner, M. K., Wei, W., Belkasim, S., Beaumont, R., Singh, S. P., Suarez, S. G., Hartswick, D., Stern, J. E., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2319641121 · Cited by 26
Nonapeptides mediate trade-offs in parental care strategy
DeAngelis, R., Dodd, L., & Rhodes, J. S. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104717 · Cited by 24
Vasopressinergic Neurocircuitry Regulating Social Attachment in a Monogamous Species
Tickerhoof, M. C., & Smith, A. S. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00265 · Cited by 26
Is there a physiological basis for the couvade and onset of paternal care?
Mason, C., & Elwood, R. (1995) · International Journal of Nursing Studies · doi:10.1016/0020-7489(94)00038-l · Cited by 24
Gammie, S. C., & Lonstein, J. S. (2005) · doi:10.1093/acprof:oso/9780195168761.003.0011 · Cited by 24
Flipping the parental switch: from killing to caring in male mammals
Elwood, R. W., & Stolzenberg, D. S. (2020) · Animal Behaviour · doi:10.1016/j.anbehav.2020.05.001 · Cited by 22
Perkeybile, A. M., & Bales, K. L. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.04.024 · Cited by 22
Examining the Role of Vasopressin in the Modulation of Parental and Sexual Behaviors
Zimmermann-Peruzatto, J. M., Lazzari, V. M., de Moura, A. C., Almeida, S., & Giovenardi, M. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00130 · Cited by 23
Bester‐Meredith, J. K., & Marler, C. A. (2012) · Brain Behavior and Evolution · doi:10.1159/000341899 · Cited by 23
McEwen (2004) · doi:10.1016/s1054-3589(04)50016-9 · Cited by 22
Auger, C. J., & Vanzo, R. J. (2005) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2005.01400.x · Cited by 21
Arginine Vasotocin Preprohormone Is Expressed in Surprising Regions of the Teleost Forebrain
Rodriguez-Santiago, M., Nguyen, J. M., Winton, L. S., Weitekamp, C. A., & Hofmann, H. A. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00195 · Cited by 22
Terleph, T. A., Jean‐Baptiste, N., & Bamshad, M. (2004) · Journal of Mammalogy · doi:10.1644/bns-108.1 · Cited by 19
Northcutt, K. V., & Lonstein, J. S. (2011) · Brain Behavior and Evolution · doi:10.1159/000326618 · Cited by 18
Oxytocin and vasopressin in non-human primates
Ragen, B., & Bales, K. L. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139017855.019 · Cited by 18
Evolutionary development of neural systems in vertebrates and beyond
O’Connell, L. A. (2013) · Journal of Neurogenetics · doi:10.3109/01677063.2013.789511 · Cited by 17
Hormonal changes in first-time human fathers in relation to paternal investment
Rilling, J. K., Lee, M., Zhou, C., Jung, E., Arrant, E. J., Davenport-Nicholson, A., Zhang, X., & Ethun, K. F. (2025) · Hormones and Behavior · doi:10.1016/j.yhbeh.2025.105740 · Cited by 18
Lee, G., & Yoon, M. (2020) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2020.106482 · Cited by 17
Oztan, O., Zyga, O., Stafford, D. E. J., & Parker, K. J. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104870 · Cited by 18
Conditioned mate-guarding behavior in the female rat
Holley, A., Shalev, S., Bellevue, S., & Pfaus, J. G. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.04.034 · Cited by 18
Cavanaugh, J., & French, J. A. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.02.006 · Cited by 15
Attachment in integrative neuroscientific perspective.
Hrubý, R., Hašto, J., & Minárik, P. (2011) · PubMed · Cited by 16
Sensitive Periods, Vasotocin-Family Peptides, and the Evolution and Development of Social Behavior
Baran, N. M. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00189 · Cited by 16
Brain Systems Underlying Social Behavior
Weitekamp, C. A., & Hofmann, H. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00025-7 · Cited by 17
Early experience and the developmental programming of oxytocin and vasopressin
Sue carter, C., Boone, E. M., & Bales, K. L. (2008) · Neurobiology of the Parental Brain · doi:10.1016/b978-012374285-8.00027-5 · Cited by 14
Taylor, J. H., Intorre, A. A., & French, J. A. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00181 · Cited by 16
Coen, C. W., Bennett, N. C., Holmes, M. M., & Faulkes, C. G. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-65943-1_3 · Cited by 16
Trezza, V., & Campolongo, P. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5193-08.2009 · Cited by 15
Panzica, G., Aste, N., Castagna, C., Balthazart, J., & Viglietti‐Panzica, C. (1997) · Springer eBooks · doi:10.1007/978-3-642-60915-2_11 · Cited by 16
Behavioral Roles of Oxytocin and Vasopressin
Benjamin, C. (2012) · InTech eBooks · doi:10.5772/50422 · Cited by 14
Ahmed, E. I., Northcutt, K. V., & Lonstein, J. S. (2011) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2011.10.006 · Cited by 13
Marler, C. A., Trainor, B. C., Gleason, E. D., Bester‐Meredith, J. K., & Becker, E. A. (2008) · Elsevier eBooks · doi:10.1016/b978-012374285-8.00028-7 · Cited by 14
MILLER, M. A., Ferris, C. F., & Kolb, P. E. (1999) · Molecular Brain Research · doi:10.1016/s0169-328x(99)00029-7 · Cited by 14
Self-citationVasopressin as Possible Treatment Option in Autism Spectrum Disorder
László, K., Vörös, D., Correia, P., Fazekas, C. L., Török, B., Plangár, I., & Zelena, D. (2023) · Biomedicines · doi:10.3390/biomedicines11102603 · Cited by 13
Social regulatory functions of vasotocin and isotocin in fish
Thompson, R. R., & Walton, J. C. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139017855.008 · Cited by 14
Chary, M., Cruz, J. P., Bardi, M., & Becker, E. A. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.05.013 · Cited by 13
Iwata, E., Nagai, Y., & Sasaki, H. (2010) · The Open Fish Science Journal · doi:10.2174/1874401x01003010147 · Cited by 12
Witte, A., de Moor, M. D., Majdandžić, M., Verhees, M., van IJzendoorn, M. H., & Bakermans-Kranenburg, M. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2022.105175 · Cited by 9
SOCIAL BIOLOGY OF RODENTS: TRENDS, CHALLENGES, AND FUTURE DIRECTIONS
Lacey, E. A., & Solomon, N. G. (2003) · Journal of Mammalogy · doi:10.1644/ble-016 · Cited by 11
Role of oxytocin and vasopressin in the transitions of weaning in the rat
Kavushansky, A., & Leshem, M. (2004) · Developmental Psychobiology · doi:10.1002/dev.20031 · Cited by 11
BAXTER, A. B., Karaskiewicz, C. L., Campbell, L. A., Kinnally, E. L., Ferrer, E. E., Seelke, A. M. H., Freeman, S. M., & Bales, K. L. (2023) · Journal of Neuroendocrinology · doi:10.1111/jne.13304 · Cited by 10
Paternal care in rodents: Ultimate causation and proximate mechanisms
Gromov, V. S. (2020) · Russian Journal of Theriology · doi:10.15298/rusjtheriol.19.1.01 · Cited by 10
Transcriptomic analysis of paternal behaviors in prairie voles
Duclot, F., Liu, Y., Saland, S. K., Wang, Z., & Kabbaj, M. (2022) · BMC Genomics · doi:10.1186/s12864-022-08912-y · Cited by 11
Self-citationGOODSON, J. L., EIBACH, R., DUKES, A., FRIEDMAN, M., SAKATA, J., THOMPSON, R., & ADKINS‐REGAN, E. (1997) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1997.tb51956.x · Cited by 10
Witte, A., Riem, M., van der Knaap, N., de Moor, M. D., van IJzendoorn, M. H., & Bakermans-Kranenburg, M. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.105731 · Cited by 8
Fricker, B. A., & Kelly, A. M. (2023) · Hormones and Behavior · doi:10.1016/j.yhbeh.2023.105462 · Cited by 9
Fang, Q., & Wang, J. (2017) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2017.03.001 · Cited by 9
Association between parental behaviors and structural plasticity in the brain of male rodents
Inada, K., & Miyamichi, K. (2023) · Neuroscience Research · doi:10.1016/j.neures.2023.06.007 · Cited by 9
Neuroendocrinology and Behavior
Sumiyoshi, T. (2012) · InTech eBooks · doi:10.5772/1666 · Cited by 9
The effects of chronic restraint stress on empathy-like behaviour in rats
Şen, A., Kara, A. Y., Koyu, A., Şimşek, F., Kızıldağ, S., & Uysal, N. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136255 · Cited by 8
Forebrain connections of medial agranular cortex in the prairie vole, Microtus ochrogaster
Reep, R. L., & Kirkpatrick, B. W. (1999) · Experimental Brain Research · doi:10.1007/s002210050741 · Cited by 8
Sexual dimorphism in the brain: It's worse than you thought
Kirkpatrick, B. W., & Bryant, N. L. (1995) · Biological Psychiatry · doi:10.1016/0006-3223(95)00359-o · Cited by 8
Social Games and Genic Selection Drive Mammalian Mating System Evolution and Speciation
Sinervo, B., Chaine, A. S., & Miles, D. B. (2019) · The American Naturalist · doi:10.1086/706810 · Cited by 7
Review: Sad dads: Paternal postpartum depression.
Kim, P., & Swain, J. E. (2007) · Cited by 7
Ziegler, T. E. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809633-8.20543-8 · Cited by 6
Hiura, L. C., Lazaro, V. A., & Ophir, A. G. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1172845 · Cited by 6
Williams, B., Northcutt, K. V., Rusanowsky, R. D., Mennella, T. A., Lonstein, J. S., & Quadros-Mennella, P. S. (2013) · Brain Research · doi:10.1016/j.brainres.2013.01.011 · Cited by 6
Vasopressin and the Neurogenetics of Parental Care
Snyder‐Mackler, N., & Tung, J. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.027 · Cited by 6
Gender-specific effects of vasopressin on human social communication: An ERP study
Wu, X., Feng, C., He, Z., Gong, X., Luo, Y., & Luo, Y. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.04.014 · Cited by 6
Mangiamele, L. A., Keeney, A. D. T., D’Agostino, E., & Thompson, R. R. (2013) · Brain Behavior and Evolution · doi:10.1159/000350589 · Cited by 6
Mayer, C., & Schalkhammer, T. G. M. (2002) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8101-2_2 · Cited by 6
The role of avpr1a microsatellite length on reproductive success of female Microtus ochrogaster
Harris, M. N., Alvarez, R. M., Keane, B., Talib, A. D., Eiswerth, M. J., & Solomon, N. G. (2014) · Behaviour · doi:10.1163/1568539x-00003178 · Cited by 5
Ben-Zaken, I., Haim, A., & Zubidat, A. E. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.089607 · Cited by 5
Do nonapeptides regulate parental care depending on experience in zebra finches?
Kelly, E. M., & Adkins–Regan, E. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.104603 · Cited by 5
Metadata
- Authors
- Wang, Z., Ferris, C. F., & De Vries, G. J.
- Affiliations
- University of Massachusetts Amherst (US)
- Department of Psychology, University of Massachusetts, Amherst 01003.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1994-01-04
- Volume
- 91
- Issue
- 1
- Pages
- 400-404
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC42955
- OpenAlex
- W1970304107
- Cited by
- 381
- References
- 29
- Citations by year
- 2026: 7 · 2025: 11 · 2024: 4 · 2023: 9 · 2022: 29 · 2021: 6 · 2020: 12 · 2019: 8 · 2018: 10 · 2017: 18 · 2016: 10 · 2015: 14 · 2014: 16 · 2013: 18 · 2012: 19
- FWCI
- 28.87
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Digital Archive @ GSU (submittedVersion)
- Counseling And Psychological Services Dissertations (Georgia State University) (submittedVersion)
- ScholarWorks@UMassAmherst (University of Massachusetts Amherst) (submittedVersion)
- Funders
- National Institute of Mental Health (R01MH47538, R01MH047538)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Behavior and Reproduction
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Keywords
- paternal behavior, Microtus ochrogaster, lateral septum, V1a receptor, vasopressin, d(CH2)5Tyr(Me)AVP, pup retrieval, social behavior, neuroendocrine regulation of behavior
- MeSH terms
- Animals, Arginine Vasopressin, Behavior, Animal, Arvicolinae, Dose-Response Relationship, Drug, Humans, Male, Paternal Behavior, Septum Pellucidum
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review